Drug intelligence / Profile preview

sintilimab + ifosfamide + carboplatin + etoposide

Development stage
Unknown
Lead developer
Suzhou Innovent Biologics
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

This is a **combination regimen** consisting of **sintilimab** (a PD-1 inhibitor/monoclonal antibody against programmed cell death protein 1), **ifosfamide** (an alkylating agent), **carboplatin** (a platinum-based chemotherapy), and **etoposide** (a topoisomerase II inhibitor). Sintilimab is an immune checkpoint inhibitor that blocks PD-1, enhancing T-cell mediated anti-tumor immune responses. The addition of sintilimab to the ICE chemotherapy regimen (ifosfamide, carboplatin, etoposide) has shown improved complete remission rates and favorable progression-free survival in patients with **relapsed or refractory classical Hodgkin lymphoma** who have failed first-line chemotherapy. The regimen was studied in a multicenter, randomized, double-blind phase 3 trial (the ORIENT-21 study) and is not approved by the US FDA; conditional approval for sintilimab monotherapy exists in China for third-line cHL. The regimen has an acceptable safety profile, with hematologic toxicities as the main adverse events[1][5][6][8].

Other names
sintilimab plus ICE
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)DNATOP2A (DNA topoisomerase II)

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